New Margin-Based Biochar for Removing Hydrogen Sulﬁde Generated during the Anaerobic Wastewater Treatment

: The present research concerns the development of a new device and process intended for the puriﬁcation and treatment of sulfurous elements, and more particularly, of hydrogen sulﬁde (H 2 S) from the biogas produced at the time of the anaerobic fermentation in the puriﬁcation stations. The controlled dumps or any other unit are likely to produce biogas with concentrations of H 2 S harmful to the operation of the machines for the valorization of the produced biogas or deodorization. This device uses new biochar from a mixture of dehydrated digested sludge from sewage treatment plants and margins from traditional crushing units, followed by biological treatment in a liquid medium at a controlled temperature. The liquid medium is based on a margin (nutrient) with culture support (large granules of biochar) in suspension by the injection under the pressure of biogas coming from the biochar ﬁlter. Physico-chemical characterization of the biochar and a test practiced on the new device of raw biogas treatment were realized. The results showed that the newly synthesized biochar has a low speciﬁc surface and a highly undeveloped porosity. The spectrum corresponding to the images of the biochar reveals the presence of C, O, N, Al, Si, P, and Fe, as signiﬁcant elements with the following respective percentages: 37.62%, 35.78%, 1.87%, 4.26%, 7.33%, 8.56%, and 4.58%. C the EDX test the prototype the invention eliminated 97% of the H 2 S from the biogas produced.


Introduction
Increasing concerns about climate change, air quality, energy import dependence, and fossil fuel depletion are increasing the demand for renewable fuels. The production site of these renewable fuels is multiple: landfills, sewage treatment plants, and industrial or food waste treatment plants [1].
Biogas results from the anaerobic digestion of organic matter by a consortium of microorganisms. It is a removable energy mainly composed of methane (CH 4 ) and carbon dioxide (CO 2 ). There are other gases such as nitrogen (N 2 ), water vapor (H 2 O), ammonia (NH 3 ), hydrogen sulfide (H 2 S), siloxanes, and other sulfur compounds.
The biogas must be cleaned (removal of H 2 S and siloxanes) and upgraded (removal of CO 2 ) to be used as an energy source (biomethane) to produce heat and electricity [2]. H 2 S in biogas is typically 50-5000 ppmv, but in some cases it can reach 20,000 ppmv (2% v/v). It is a colorless, flammable, and foul-smelling toxic gas.
This contaminant is known for its undesirable odor and is transformed into sulfur dioxide (SO 2 ) and sulfuric acid (H 2 SO 4 ), which are highly corrosive and dangerous for health and the environment. Its elimination is essential for any possible use of biogas [3][4][5].
According to several authors, sewage sludge is a problematic waste and a valuable raw material for producing biogas and biochar by thermal conversion which is an environmentally friendly alternative [6][7][8].
Nevertheless, the biogas produced contains impurities that make its direct use in machines of valorization, either thermal or electric energy. Almost impossible or comes back to too expensive maintenance costs were to the necessity to purify the produced biogas of the sulfurous elements in general and the hydrogen sulfide H 2 S, especially before its use. The operating costs and/or unpredictably high H 2 S efficiencies [9][10][11].
The present article refers to the treatment and purification of anaerobic digestion gases. More particularly for a device, this is a process for purification and treatment of sulfurous elements in the biogas produced by anaerobic digestion, especially hydrogen sulfide H 2 S.
"Biochar" is a recently coined term emerging in conjunction with renewable fuel and carbon sequestration. It is another carbon-based material that is produced by a combination of pyrolysis (limited amount of oxygen) and thermal degradation of organic material at temperatures between 100-700 • C [12][13][14]. Several recent types of research have worked on directly adding biochar to anaerobic digestion systems. Unfortunately, they have focused on improving CH 4 production but have not addressed the effect of biochar addition on H 2 S production [15][16][17]. Shen et al. (2015) added corn stover-based biochar directly to an anaerobic digester treating municipal wastewater, resulting in biogas production with over 90% CH 4 and less than five parts per billion H 2 S [18]. Another study used pine and white oak biochar in digesters to increase the percentage of CH 4 in the biogas stream [17].
Studies have been carried out on the development of a multifunctional, efficient, and durable membrane for long-term use in the treatment of complex oily wastewater [19,20]. To our knowledge, there is no study on using biochar formed from wastewater treatment plant sludge and margins for H 2 S reduction.
The origin of this work concerns the development of a new device and process designed for the purification and treatment of sulfurous elements in biogas using sludge from the wastewater treatment plant and the margins as a source of biochar production.
The main objectives of this work involve: i. Valorizing sludge from sewage treatment plants and margins (source of pollution). ii. Reduction in the costs of consumables by using the mixture of sludge and margins as raw material to produce biochar as adsorbent.

Biochar Production
The slow pyrolysis produces the biochar in the absence of oxygen at a temperature between 400 and 500 • C for a minimum of 4 h, using a dried mixture of digested and dehydrated sewage plant sludge (80% dryness) with raw margins from the crushing of olive oil. After mixing the sludge and the margin, a second natural drying is carried out to bring the dryness of the mixture back to 80% before starting the pyrolysis to produce the biochar (final product, as shown in Figure 1) [21][22][23]. to bring the dryness of the mixture back to 80% before starting the pyrolysis to produce the biochar (final product, as shown in Figure 1) [21][22][23].

Physicochemical Characterization of Biochar
Infrared (IR) spectroscopy was used to characterize the biochar. The IR spectra illustrate the bond stretches in the organic functional groups on the biochar surface [24].
The thermal stability of this material was identified by ATG thermogravimetric analysis with a heating rate of 10 °C/min up to a temperature of 800 °C under gas (nitrogen) sweep [25].
The pore size distribution and surface characteristics of the prepared biochar were measured by N2 gas adsorption-desorption at the temperature of liquid N2 (−195.85 °C). The Brunauer determined the specific surface areas-Emmett-Teller (BET) method. Inductively coupled plasma spectrometry was used for the characterization of inorganic constituents of the biochar sample. The analysis was used to identify the metals in the samples (Mg, Al, Si, P, Ca, Mn, Fe, Ni, Cu, Zn, Na, B, Co, Pb, and Cd) and to measure the content of these elements [26,27].
The surface morphology and distribution of the chemical elements of biochar were studied by scanning electron microscopy (SEM). SEM images of biochars were obtained using a Gemini SEM 500-8203017153 scanning electron microscope (SEM) with an accelerating voltage of 3.00 kV [28].

Description of the Pilot
Several pilots were set up during this experiment to test the H2S adsorption capacities of the materials studied.
The whole device of desulfurization of the anaerobic digestion biogas by biochar filter and drowned reactor based on margin with suspension culture is formed of ( Figure 2): ✓ A biochar filter (2) whose biochar is produced from a mixture of sewage plant sludge and margin used as an adsorbent for the pre-filtration of sulfur compounds in biogas and, more particularly, hydrogen sulfide (H2S). ✓ Hydraulic guard (5) to ensure minimum hydraulic pressure through the biochar filter and can serve as an additional biological treatment reactor.

Physicochemical Characterization of Biochar
Infrared (IR) spectroscopy was used to characterize the biochar. The IR spectra illustrate the bond stretches in the organic functional groups on the biochar surface [24].
The thermal stability of this material was identified by ATG thermogravimetric analysis with a heating rate of 10 • C/min up to a temperature of 800 • C under gas (nitrogen) sweep [25].
The pore size distribution and surface characteristics of the prepared biochar were measured by N 2 gas adsorption-desorption at the temperature of liquid N 2 (−195.85 • C). The Brunauer determined the specific surface areas-Emmett-Teller (BET) method. Inductively coupled plasma spectrometry was used for the characterization of inorganic constituents of the biochar sample. The analysis was used to identify the metals in the samples (Mg, Al, Si, P, Ca, Mn, Fe, Ni, Cu, Zn, Na, B, Co, Pb, and Cd) and to measure the content of these elements [26,27].
The surface morphology and distribution of the chemical elements of biochar were studied by scanning electron microscopy (SEM). SEM images of biochars were obtained using a Gemini SEM 500-8203017153 scanning electron microscope (SEM) with an accelerating voltage of 3.00 kV [28].

Description of the Pilot
Several pilots were set up during this experiment to test the H 2 S adsorption capacities of the materials studied.
The whole device of desulfurization of the anaerobic digestion biogas by biochar filter and drowned reactor based on margin with suspension culture is formed of ( Figure 2): to bring the dryness of the mixture back to 80% before starting the pyrolysis to produce the biochar (final product, as shown in Figure 1) [21][22][23].

Physicochemical Characterization of Biochar
Infrared (IR) spectroscopy was used to characterize the biochar. The IR spectra illustrate the bond stretches in the organic functional groups on the biochar surface [24].
The thermal stability of this material was identified by ATG thermogravimetric analysis with a heating rate of 10 °C/min up to a temperature of 800 °C under gas (nitrogen) sweep [25].
The pore size distribution and surface characteristics of the prepared biochar were measured by N2 gas adsorption-desorption at the temperature of liquid N2 (−195.85 °C). The Brunauer determined the specific surface areas-Emmett-Teller (BET) method. Inductively coupled plasma spectrometry was used for the characterization of inorganic constituents of the biochar sample. The analysis was used to identify the metals in the samples (Mg, Al, Si, P, Ca, Mn, Fe, Ni, Cu, Zn, Na, B, Co, Pb, and Cd) and to measure the content of these elements [26,27].
The surface morphology and distribution of the chemical elements of biochar were studied by scanning electron microscopy (SEM). SEM images of biochars were obtained using a Gemini SEM 500-8203017153 scanning electron microscope (SEM) with an accelerating voltage of 3.00 kV [28].

Description of the Pilot
Several pilots were set up during this experiment to test the H2S adsorption capacities of the materials studied.
The whole device of desulfurization of the anaerobic digestion biogas by biochar filter and drowned reactor based on margin with suspension culture is formed of ( Figure 2): ✓ A biochar filter (2) whose biochar is produced from a mixture of sewage plant sludge and margin used as an adsorbent for the pre-filtration of sulfur compounds in biogas and, more particularly, hydrogen sulfide (H2S). ✓ Hydraulic guard (5) to ensure minimum hydraulic pressure through the biochar filter and can serve as an additional biological treatment reactor.
A biochar filter (2) whose biochar is produced from a mixture of sewage plant sludge and margin used as an adsorbent for the pre-filtration of sulfur compounds in biogas and, more particularly, hydrogen sulfide (H 2 S). to bring the dryness of the mixture back to 80% before starting the pyrolysis to produce the biochar (final product, as shown in Figure 1) [21][22][23].

Physicochemical Characterization of Biochar
Infrared (IR) spectroscopy was used to characterize the biochar. The IR spectra illustrate the bond stretches in the organic functional groups on the biochar surface [24].
The thermal stability of this material was identified by ATG thermogravimetric analysis with a heating rate of 10 °C/min up to a temperature of 800 °C under gas (nitrogen) sweep [25].
The pore size distribution and surface characteristics of the prepared biochar were measured by N2 gas adsorption-desorption at the temperature of liquid N2 (−195.85 °C). The Brunauer determined the specific surface areas-Emmett-Teller (BET) method. Inductively coupled plasma spectrometry was used for the characterization of inorganic constituents of the biochar sample. The analysis was used to identify the metals in the samples (Mg, Al, Si, P, Ca, Mn, Fe, Ni, Cu, Zn, Na, B, Co, Pb, and Cd) and to measure the content of these elements [26,27].
The surface morphology and distribution of the chemical elements of biochar were studied by scanning electron microscopy (SEM). SEM images of biochars were obtained using a Gemini SEM 500-8203017153 scanning electron microscope (SEM) with an accelerating voltage of 3.00 kV [28].

Description of the Pilot
Several pilots were set up during this experiment to test the H2S adsorption capacities of the materials studied.
The whole device of desulfurization of the anaerobic digestion biogas by biochar filter and drowned reactor based on margin with suspension culture is formed of ( Figure 2): ✓ A biochar filter (2) whose biochar is produced from a mixture of sewage plant sludge and margin used as an adsorbent for the pre-filtration of sulfur compounds in biogas and, more particularly, hydrogen sulfide (H2S). ✓ Hydraulic guard (5) to ensure minimum hydraulic pressure through the biochar filter and can serve as an additional biological treatment reactor.
Hydraulic guard (5) to ensure minimum hydraulic pressure through the biochar filter and can serve as an additional biological treatment reactor.

Statistical Analysis
To confirm our outcome reliability and reproducibility, we compared the mean values of each parameter (H 2 S and CH 4 ) upstream and downstream for our anaerobic digestion biogas desulfurization system by biochar filter, using the two-sample t-test at p < 0.05 with Minitab19.1.

Statistical Analysis
To confirm our outcome reliability and reproducibility, we compared the mean values of each parameter (H2S and CH4) upstream and downstream for our anaerobic digestion biogas desulfurization system by biochar filter, using the two-sample t-test at p < 0.05 with Minitab19.1.

Physicochemical Characterization of Biochar
The type of functional groups present on the surface of the biochar is crucial because they generally improve its adsorption abilities. Indeed, the presence of specific functional groups such as hydroxyl groups or the presence of water in the biochar favors the formation of an aqueous film on the surface of the biochar allowing the dissociation of hydrogen sulfide into HS. The IR spectrum of the biochar is shown in Figure 3. Several bands characteristic of different groups can be distinguished (Figure 3a).
A band located at 3365 cm −1 , characteristic of the elongation of O-H bonds, can be observed on the infrared spectrum ( Figure 3b). This band of weak intensity informs the number of hydroxyl groups on the surface. It has been previously found that many free hydroxyl groups and structural hydroxyl groups (-COOH and -COH) decompose during the pyrolysis of the sludge [29]. Indeed, the mass loss found in a temperature range below 200 °C was only 3%, indicating the low water content of the material. The band observed at 2923 cm −1 is characteristic of elongations of aliphatic C-H bonds, while the band observed at 1794 cm −1 indicates the presence of carbonyl groups on the biochar surface. The intense band observed at 1427 can be attributed to C-H bond deformations. It is well established that the region between 400 cm −1 and 1500 cm −1 in an IR spectrum is known as the fingerprint region. It usually contains many peaks, making it difficult to identify individual peaks. However, the fingerprint region of a given compound is unique and, therefore, can be used to distinguish between compounds.
From the ICP results, we found that the material is composed of several elements such as Ca, P, Al, and Si, at a level greater than 20%. These elements are likely to form stable mineral phases at high temperatures, so an exact assignment of the different peaks

Physicochemical Characterization of Biochar
The type of functional groups present on the surface of the biochar is crucial because they generally improve its adsorption abilities. Indeed, the presence of specific functional groups such as hydroxyl groups or the presence of water in the biochar favors the formation of an aqueous film on the surface of the biochar allowing the dissociation of hydrogen sulfide into HS. The IR spectrum of the biochar is shown in Figure 3. Several bands characteristic of different groups can be distinguished (Figure 3a).  Thermogravimetric analysis was used to evaluate the thermal stability of the synthesized biochar. The thermogravimetric analysis was performed under air by heating the biochar at 10 °C/min to 800 °C. Figure 4 shows a mass loss of about 3% at a temperature of about 200 °C. This first mass loss corresponds to the dehydration of the biochar or decomposition of the oxygenated groups present on the material's surface. The mass loss observed after 200 °C, of 29%, corresponds to the decomposition and degradation of impurities, volatile matter, and carbon, mainly into CO and CO2. The total mass loss found for the biochar is in the order of 33%, indicating that the carbon content of the material is A band located at 3365 cm −1 , characteristic of the elongation of O-H bonds, can be observed on the infrared spectrum (Figure 3b). This band of weak intensity informs the number of hydroxyl groups on the surface. It has been previously found that many free hydroxyl groups and structural hydroxyl groups (-COOH and -COH) decompose during the pyrolysis of the sludge [29]. Indeed, the mass loss found in a temperature range below Water 2022, 14, 3319 5 of 12 200 • C was only 3%, indicating the low water content of the material. The band observed at 2923 cm −1 is characteristic of elongations of aliphatic C-H bonds, while the band observed at 1794 cm −1 indicates the presence of carbonyl groups on the biochar surface. The intense band observed at 1427 can be attributed to C-H bond deformations. It is well established that the region between 400 cm −1 and 1500 cm −1 in an IR spectrum is known as the fingerprint region. It usually contains many peaks, making it difficult to identify individual peaks. However, the fingerprint region of a given compound is unique and, therefore, can be used to distinguish between compounds.
From the ICP results, we found that the material is composed of several elements such as Ca, P, Al, and Si, at a level greater than 20%. These elements are likely to form stable mineral phases at high temperatures, so an exact assignment of the different peaks observed on the infrared spectrum in the fingerprint region becomes difficult due to the complex composition of the biochar.
Thermogravimetric analysis was used to evaluate the thermal stability of the synthesized biochar. The thermogravimetric analysis was performed under air by heating the biochar at 10 • C/min to 800 • C. Figure 4 shows a mass loss of about 3% at a temperature of about 200 • C. This first mass loss corresponds to the dehydration of the biochar or decomposition of the oxygenated groups present on the material's surface. The mass loss observed after 200 • C, of 29%, corresponds to the decomposition and degradation of impurities, volatile matter, and carbon, mainly into CO and CO 2 . The total mass loss found for the biochar is in the order of 33%, indicating that the carbon content of the material is relatively low. Therefore, the residue of 67% remaining at 800 • C indicates the presence of mineral phases that form under air at 800 • C. The results concerning the thermal stability of biochar, obtained by pyrolysis of a mixture of sludge and margin, are comparable to that of biochar obtained by pyrolysis of pigeon pea stems at 600 • C [30].
observed on the infrared spectrum in the fingerprint region becomes difficult due to the complex composition of the biochar. Thermogravimetric analysis was used to evaluate the thermal stability of the synthesized biochar. The thermogravimetric analysis was performed under air by heating the biochar at 10 °C/min to 800 °C. Figure 4 shows a mass loss of about 3% at a temperature of about 200 °C. This first mass loss corresponds to the dehydration of the biochar or decomposition of the oxygenated groups present on the material's surface. The mass loss observed after 200 °C, of 29%, corresponds to the decomposition and degradation of impurities, volatile matter, and carbon, mainly into CO and CO2. The total mass loss found for the biochar is in the order of 33%, indicating that the carbon content of the material is relatively low. Therefore, the residue of 67% remaining at 800 °C indicates the presence of mineral phases that form under air at 800 °C. The results concerning the thermal stability of biochar, obtained by pyrolysis of a mixture of sludge and margin, are comparable to that of biochar obtained by pyrolysis of pigeon pea stems at 600 °C [30]. In order to identify the composition of the biochar and the different mineral phases likely to have been formed after the thermogravimetric analysis at 800 °C, we used ICP. Table 1 shows all biochar's metallic and non-metallic elements and their concentrations. This table also compares the attention of the features in the biochar to the allowable levels of contaminants in biochar as defined by the International Biochar Initiative (IBI), the British Biochar Foundation (BQM), and the European Biochar Foundation (EBC) [31]. In order to identify the composition of the biochar and the different mineral phases likely to have been formed after the thermogravimetric analysis at 800 • C, we used ICP. Table 1 shows all biochar's metallic and non-metallic elements and their concentrations. This table also compares the attention of the features in the biochar to the allowable levels of contaminants in biochar as defined by the International Biochar Initiative (IBI), the British Biochar Foundation (BQM), and the European Biochar Foundation (EBC) [31]. The results obtained from the ICP analysis show that the biochar contains high concentrations of Ca, Mg, Al, P, and Fe. The majority of elements comprising the biochar are calcium, with 14%, followed by phosphorus and aluminum, with percentages of about 2.14% and 2.13%, respectively. The biochar being rich in mineral elements and heteroatoms such as P and B explains the subsistence of a residue of about 67% after calcination under air at 800 • C. The high Ca content of the biochar can be explained by the liming of the sludge generally carried out to stabilize it.
The synthesized biochar has a dense structure, and no porosity can be appreciated at different magnifications (Figure 5a-c). By grinding the biochar, particles of the order of 17 µm in size were obtained (Figure 5b). Furthermore, at magnifications on the order of ×11,500, the material appears to possess a rough structure, probably due to mineral phase aggregates. The composition of the material was determined by energy dispersive X-ray spectroscopy (EDS). In Figure 5k, the spectrum corresponding to the biochar images reveals the presence of C, O, N, Al, Si, P, and Fe, as the majority elements with the following respective percentages: 37.62%, 35.78%, 1.87%, 4.26%, 7.33%, 8.56%, and 4.58%. It is important to note that the C content of the synthesized biochar found by EDX is quite comparable to that estimated from GTA. The SEM-EDS images of the biochar (Figure 5d-j) reveal the homogeneous distribution of the different elements on the biochar surface.
The exact composition of sludge varies according to the origin of the wastewater, the time of year, and the type of treatment and conditioning practiced in the treatment plant. The waste sludge represents, above all, a raw material composed of different elements (organic matter, fertilizing elements (N and P), metallic trace elements, organic trace elements, and pathogens) [32].
The concentration of organic matter can vary from 30 to 80%. The organic matter of the sludge is constituted by particles that have been eliminated by gravity. Lipids represent 6 to 19% of the organic matter, polysaccharides, proteins, and amino acids represent up to 33% of the organic matter. Thus, we find the products of metabolization and microbial bodies resulting from biological treatments (digestion, stabilization) [31]. Water 2022, 14, x FOR PEER REVIEW 7 of 12 The nature and concentration of organic and inorganic pollutants in wastewater depend on the activities connected to the network [33]. Most of the chemical contamination comes from industrial discharges and, to a lesser extent, from domestic discharges (use of solvents, do-it-yourself waste, detergent) [34]. Due to the settling during treatment, these chemical contaminants are found in the sludge in very high concentrations compared to wastewater.
The knowledge of the specific surface, the pore volume, and the pore size define the biochar structure. The ability of these properties is of great importance because they help to explain the accessibility of the surface to adsorbates related to the shape and size of the pores and, consequently, its adsorption ability. The nitrogen adsorption isotherm is plotted by plotting the amount adsorbed per gram of adsorbent against relative pressure. The nitrogen adsorption curve for biochar is shown in Figure 6. From the figure, it can be seen that the isotherm obtained for the biochar is type II. Type II isotherms are typically received on non-porous or macroporous materials, where monolayers and multilayers form on the surface [35].
The result obtained is in perfect agreement with the scanning electron microscopy. Indeed, in the SEM pictures, we noticed that the material does not present any porosity and that the observed structure is relatively dense. The synthesized biochar has a low The nature and concentration of organic and inorganic pollutants in wastewater depend on the activities connected to the network [33]. Most of the chemical contamination comes from industrial discharges and, to a lesser extent, from domestic discharges (use of solvents, do-it-yourself waste, detergent) [34]. Due to the settling during treatment, these chemical contaminants are found in the sludge in very high concentrations compared to wastewater.
The knowledge of the specific surface, the pore volume, and the pore size define the biochar structure. The ability of these properties is of great importance because they help to explain the accessibility of the surface to adsorbates related to the shape and size of the pores and, consequently, its adsorption ability. The nitrogen adsorption isotherm is plotted by plotting the amount adsorbed per gram of adsorbent against relative pressure. The nitrogen adsorption curve for biochar is shown in Figure 6. From the figure, it can be seen that the isotherm obtained for the biochar is type II. Type II isotherms are typically received on non-porous or macroporous materials, where monolayers and multilayers form on the surface [35]. specific surface and a highly undeveloped porosity explaining the obtaining of a type II isotherm characteristic of materials with no porosity. From the results of monitoring the biogas treatment in a device, it is found that the concentration of hydrogen sulfide in the raw biogas is 5000 ppm upstream. Moreover, this biogas downstream of the treatment device is about 131 ppm after 38 days of treatment (Figure 7).  The result obtained is in perfect agreement with the scanning electron microscopy. Indeed, in the SEM pictures, we noticed that the material does not present any porosity and that the observed structure is relatively dense. The synthesized biochar has a low specific surface and a highly undeveloped porosity explaining the obtaining of a type II isotherm characteristic of materials with no porosity.
From the results of monitoring the biogas treatment in a device, it is found that the concentration of hydrogen sulfide in the raw biogas is 5000 ppm upstream. Moreover, this biogas downstream of the treatment device is about 131 ppm after 38 days of treatment ( Figure 7). specific surface and a highly undeveloped porosity explaining the obtaining of a type II isotherm characteristic of materials with no porosity. From the results of monitoring the biogas treatment in a device, it is found that the concentration of hydrogen sulfide in the raw biogas is 5000 ppm upstream. Moreover, this biogas downstream of the treatment device is about 131 ppm after 38 days of treatment (Figure 7).   A study was carried out on H 2 S adsorption with non-hazardous waste incineration bottom ash and was mainly studied with natural biogas. The reactors were more significant than those used for biochars, and the experiments lasted longer. Adsorption capacities ranged from 3 to 298 mgH 2 S/g material. The lowest value was obtained with dry biogas, and 15% moistened MIDND.
The flow rate necessary for the sizing of the biochar filter, and in order to have the targeted results (minimum abatement of 90%) for a raw biogas concentration of 5000 ppm of hydrogen sulfide, is 0.5 m 3 /h of biogas for a biochar volume of 30 L and a volume of 20 L for the biological reactor for the same flow rate.
The results shown in Figure 8 represent the comparison between the average values of each parameter of H 2 S and CH 4 in the anaerobic digestion biogas desulphurization system upstream and downstream by the BIOCHAR filter. The ( Figure 8A) shows a crucial decrease in the amount of H 2 S between the front and back of our system (p < 0.05). While the amount of CH 4 shows no difference between upstream and downstream ( Figure 8B). This difference allows us to confirm the efficiency of our prototype in reducing the hydrogen sulfide generated during the anaerobic wastewater treatment. A study was carried out on H2S adsorption with non-hazardous waste incineration bottom ash and was mainly studied with natural biogas. The reactors were more significant than those used for biochars, and the experiments lasted longer. Adsorption capacities ranged from 3 to 298 mgH2S/g material. The lowest value was obtained with dry biogas, and 15% moistened MIDND.
The flow rate necessary for the sizing of the biochar filter, and in order to have the targeted results (minimum abatement of 90%) for a raw biogas concentration of 5000 ppm of hydrogen sulfide, is 0.5 m 3 /h of biogas for a biochar volume of 30 L and a volume of 20 L for the biological reactor for the same flow rate.
The results shown in Figure 8 represent the comparison between the average values of each parameter of H2S and CH4 in the anaerobic digestion biogas desulphurization system upstream and downstream by the BIOCHAR filter. The ( Figure 8A) shows a crucial decrease in the amount of H2S between the front and back of our system (p < 0.05). While the amount of CH4 shows no difference between upstream and downstream ( Figure 8B). This difference allows us to confirm the efficiency of our prototype in reducing the hydrogen sulfide generated during the anaerobic wastewater treatment. The particularity of this device and process is that it allows treating a wide range of biogas produced in anaerobic digestion systems while ensuring highly efficient yields with short residence times, valorizing the harmful by-products coming from the sewage treatment plants (sludge) and the crushing of olives (margin), posing problems for the sewage treatment plants and for the natural environment. This allows the minimizing of the expenses on the consumables used in the prior art processes, activated carbons, minerals, and nutrients for the biomass with easy exploitation for maximum safety.
Biochar used in this study was rich in mineral elements. It is likely that the minerals in the biochar contribute to H2S removal. Mineral content (from EDS analysis) and speciation (from ICP-OES analysis) are essential factors to consider, as metal oxides such as Ca, Mg, Al, and Fe and other elements such as P can act as H2S adsorption sites and catalytic oxidation to convert H2S to elemental sulfur and sulfates. This mainly explains the observed abatement rates and H2S removal ability by the biochar used [36]. Indeed, studies on biochar substrates prepared from anaerobically digested sewage sludge and fiber have highlighted the importance of surface alkalinity in H2S removal, as the alkaline nature was suspected to facilitate H2S dissociation [37].
Several studies have been carried out on H2S absorption using processes for removing hydrogen sulfide species from biogas by a carbon absorption material produced from dewatered and dried sewage sludge by adding mineral oil before pyrolysis. Adding mineral oil is an extra step compared to the biochar production process and an additional charge The particularity of this device and process is that it allows treating a wide range of biogas produced in anaerobic digestion systems while ensuring highly efficient yields with short residence times, valorizing the harmful by-products coming from the sewage treatment plants (sludge) and the crushing of olives (margin), posing problems for the sewage treatment plants and for the natural environment. This allows the minimizing of the expenses on the consumables used in the prior art processes, activated carbons, minerals, and nutrients for the biomass with easy exploitation for maximum safety.
Biochar used in this study was rich in mineral elements. It is likely that the minerals in the biochar contribute to H 2 S removal. Mineral content (from EDS analysis) and speciation (from ICP-OES analysis) are essential factors to consider, as metal oxides such as Ca, Mg, Al, and Fe and other elements such as P can act as H 2 S adsorption sites and catalytic oxidation to convert H 2 S to elemental sulfur and sulfates. This mainly explains the observed abatement rates and H 2 S removal ability by the biochar used [36]. Indeed, studies on biochar substrates prepared from anaerobically digested sewage sludge and fiber have highlighted the importance of surface alkalinity in H 2 S removal, as the alkaline nature was suspected to facilitate H 2 S dissociation [37].
Several studies have been carried out on H 2 S absorption using processes for removing hydrogen sulfide species from biogas by a carbon absorption material produced from dewatered and dried sewage sludge by adding mineral oil before pyrolysis. Adding mineral oil is an extra step compared to the biochar production process and an additional charge that will increase the cost of the product with a lower abatement rate than that obtained by our device [38,39]. Even heat treatment alone is not sufficient for preparing a carbon absorbent.
In our study, we succeeded in combining the filtration of biogas doped with 2 to 5% oxygen on biochar support produced from a mixture of digested and dehydrated sewage sludge and margins from a traditional crushing unit. Followed by biological treatment in liquid medium at controlled temperature, the medium is based on margin (nutrient) with culture support (large granule of biochar) in suspension by the injection under the biogas pressure from the biochar filter.
The flooded reactor for the biological treatment of sulfur compounds in biogas is an innovation; the reactor is a mixture of diluted margin and culture media for the purifying biomass at adjustable temperature. The bubbling ensures the biomass's suspension and the medium's agitation due to the biogas injected under pressure at the bottom of the flooded biological reactor.
The bacterial flows in suspension fixed on the granules of biochar (suspension support) ensure the elimination is ensured after that. The nutrition of this biomass is brought by the margin, which is the base of the solution of the biological reactor (the use of conventional nutrients is also possible); the final product is biogas in conformity with use.

Conclusions
A new adsorption process for hydrogen sulfide removal from biogas by margin-based biochar was tested on a pilot scale. Results showed that this biochar is characterized by a dense and mineral-rich structure. It is likely that these biochar minerals can act as H 2 S adsorption and catalytic oxidation sites to convert up to 98% of the H 2 S to elemental sulfur and sulfates.
The process has shown promise and further experimental work is underway to refine the new treatment device, which will be investigated, and reported in a subsequent publication.